Please use this identifier to cite or link to this item: http://hdl.handle.net/1893/35729
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dc.contributor.authorPrzulj, Dunjaen_UK
dc.contributor.authorPesola, Francescaen_UK
dc.contributor.authorMyers Smith, Katieen_UK
dc.contributor.authorMcRobbie, Haydenen_UK
dc.contributor.authorColeman, Timen_UK
dc.contributor.authorLewis, Sarahen_UK
dc.contributor.authorGriffith, Christopheren_UK
dc.contributor.authorWalton, Roberten_UK
dc.contributor.authorWhitemore, Rachelen_UK
dc.contributor.authorClark, Mirandaen_UK
dc.contributor.authorUssher, Michaelen_UK
dc.contributor.authorSinclair, Lesleyen_UK
dc.contributor.authorSeager, Emilyen_UK
dc.contributor.authorCooper, Sueen_UK
dc.contributor.authorBauld, Lindaen_UK
dc.date.accessioned2024-02-22T01:11:15Z-
dc.date.available2024-02-22T01:11:15Z-
dc.date.issued2023-07-01en_UK
dc.identifier.urihttp://hdl.handle.net/1893/35729-
dc.description.abstractBackground Some pregnant smokers try e-cigarettes, but effectiveness and safety of such use are unknown. Objectives To compare effectiveness and safety of nicotine patches and e-cigarettes in pregnancy. Design A pragmatic multi-centre randomised controlled trial. Setting Twenty-three hospitals across England, and a Stop Smoking Service in Scotland. Participants One thousand one hundred and forty pregnant daily smokers (12–24 weeks’ gestation) motivated to stop smoking, with no strong preference for using nicotine patches or e-cigarettes. Interventions Participants in the e-cigarette arm were posted a refillable e-cigarette device with two 10 ml bottles of tobacco-flavoured e-liquid (18 mg nicotine). Participants in the nicotine patches arm were posted a 2-week supply of 15 mg/16-hour nicotine patches. Supplies were provided for up to 8 weeks. Participants sourced further supplies themselves as needed. Participants in both arms received support calls prior to their target quit date, on the quit date, and weekly for the next 4 weeks. Outcome measures The primary outcome was validated prolonged abstinence at the end of pregnancy. Participants lost to follow-up or not providing biochemical validation were included as non-abstainers. Secondary outcomes included self-reported abstinence at different time points, treatment adherence and safety outcomes. Results Only 55% of self-reported abstainers mailed back useable saliva samples. Due to this, validated sustained abstinence rates were low (6.8% vs. 4.4% in the e-cigarettes and nicotine patches arms, respectively, risk ratio = 1.55, 95% confidence interval 0.95 to 2.53; Bayes factor = 2.7). In a pre-specified sensitivity analysis that excluded abstainers using non-allocated products, the difference became significant (6.8% vs. 3.6%, risk ratio = 1.93, 95% confidence interval 1.14 to 3.26; Bayes factor = 10). Almost a third of the sample did not set a target quit date and the uptake of support calls was low, as was the initial product use. At end of pregnancy, 33.8% versus 5.6% of participants were using their allocated product in the e-cigarettes versus nicotine patches arm (risk ratio = 6.01, 95% confidence interval 4.21 to 8.58). Regular use of e-cigarettes in the nicotine patches arm was more common than use of nicotine replacement products in the e-cigarette arm (17.8% vs. 2.8%). Rates of adverse events and adverse birth outcomes were similar in the two study arms, apart from participants in the e-cigarette arm having fewer infants with low birthweight (<2500 g) (9.6% vs. 14.8%, risk ratio = 0.65, 95% confidence interval 0.47 to 0.90; Bayes factor = 10.3). Limitations Low rates of validation reduced the study power. A substantial proportion of participants did not use the support on offer sufficiently to test its benefits. Sample size may have been too small to detect differences in less frequent adverse effects. Conclusions E-cigarettes were not significantly more effective than nicotine patches in the primary analysis, but when e-cigarettes use in the nicotine patches arm was accounted for, e-cigarettes were almost twice as effective as patches in all abstinence outcomes. In pregnant smokers seeking help, compared to nicotine patches, e-cigarettes are probably more effective, do not pose more risks to birth outcomes assessed in this study and may reduce the incidence of low birthweight. Future work Routine monitoring of smoking cessation and birth outcomes in pregnant women using nicotine patches and e-cigarettes and further studies are needed to confirm these results. Trial registration This trial is registered as ISRCTN62025374 and Eudract 2017-001237-65. Funding This project was funded by the National Institute for Health and Care Research (NIHR) Health Technology Assessment programme and will be published in full in Health Technology Assessment; Vol. 27, No. 13. See the NIHR Journals Library website for further project informationen_UK
dc.language.isoenen_UK
dc.publisherNational Institute for Health and Care Researchen_UK
dc.relationPrzulj D, Pesola F, Myers Smith K, McRobbie H, Coleman T, Lewis S, Griffith C, Walton R, Whitemore R, Clark M, Ussher M, Sinclair L, Seager E, Cooper S & Bauld L (2023) Helping pregnant smokers quit: a multi-centre randomised controlled trial of electronic cigarettes versus nicotine replacement therapy. <i>Health Technology Assessment</i>, 27 (13), pp. 1-53. https://doi.org/10.3310/agth6901en_UK
dc.rightsCopyright © 2023 Przulj et al. This work was produced by Przulj et al. under the terms of a commissioning contract issued by the Secretary of State for Health and Social Care. This is an Open Access publication distributed under the terms of the Creative Commons Attribution CC BY 4.0 licence, which permits unrestricted use, distribution, reproduction and adaption in any medium and for any purpose provided that it is properly attributed. See: https://creativecommons.org/licenses/by/4.0/. For attribution the title, original author(s), the publication source – NIHR Journals Library, and the DOI of the publication must be cited.en_UK
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/en_UK
dc.subjectHealth Policyen_UK
dc.titleHelping pregnant smokers quit: a multi-centre randomised controlled trial of electronic cigarettes versus nicotine replacement therapyen_UK
dc.typeJournal Articleen_UK
dc.identifier.doi10.3310/agth6901en_UK
dc.identifier.pmid37840301en_UK
dc.citation.jtitleHealth Technology Assessmenten_UK
dc.citation.issn2046-4924en_UK
dc.citation.issn1366-5278en_UK
dc.citation.volume27en_UK
dc.citation.issue13en_UK
dc.citation.spage1en_UK
dc.citation.epage53en_UK
dc.citation.publicationstatusPublisheden_UK
dc.citation.peerreviewedRefereeden_UK
dc.type.statusVoR - Version of Recorden_UK
dc.contributor.funderNational Institute for Health Researchen_UK
dc.author.emailaileen.paton@stir.ac.uken_UK
dc.description.notesAdditional authors: Felix Naughton; Peter Sasieni; Isaac Manyonda; Peter Hajeken_UK
dc.contributor.affiliationQueen Mary, University of Londonen_UK
dc.contributor.affiliationQueen Mary, University of Londonen_UK
dc.contributor.affiliationQueen Mary, University of Londonen_UK
dc.contributor.affiliationUniversity of New South Walesen_UK
dc.contributor.affiliationUniversity of Nottinghamen_UK
dc.contributor.affiliationUniversity of Nottinghamen_UK
dc.contributor.affiliationQueen Mary, University of Londonen_UK
dc.contributor.affiliationQueen Mary, University of Londonen_UK
dc.contributor.affiliationUniversity of Nottinghamen_UK
dc.contributor.affiliationUniversity of Nottinghamen_UK
dc.contributor.affiliationSt George's, University of Londonen_UK
dc.contributor.affiliationUniversity of Edinburghen_UK
dc.contributor.affiliationQueen Mary, University of Londonen_UK
dc.contributor.affiliationUniversity of Nottinghamen_UK
dc.contributor.affiliationUniversity of Edinburghen_UK
dc.identifier.isiWOS:001092584800001en_UK
dc.identifier.scopusid2-s2.0-85168267180en_UK
dc.identifier.wtid1967031en_UK
dc.contributor.orcid0000-0003-1133-8835en_UK
dc.contributor.orcid0000-0002-2054-7930en_UK
dc.contributor.orcid0000-0003-1837-3924en_UK
dc.contributor.orcid0000-0002-7777-1845en_UK
dc.contributor.orcid0000-0002-7303-4805en_UK
dc.contributor.orcid0000-0001-5308-6619en_UK
dc.contributor.orcid0000-0001-7935-8694en_UK
dc.contributor.orcid0000-0001-7700-1907en_UK
dc.contributor.orcid0000-0002-7599-8640en_UK
dc.contributor.orcid0000-0002-6179-046Xen_UK
dc.contributor.orcid0000-0002-0995-7955en_UK
dc.contributor.orcid0000-0002-2210-8181en_UK
dc.contributor.orcid0000-0001-6672-5555en_UK
dc.contributor.orcid0000-0002-1994-6395en_UK
dc.date.accepted2023-07-01en_UK
dcterms.dateAccepted2023-07-01en_UK
dc.date.filedepositdate2024-02-16en_UK
rioxxterms.apcnot requireden_UK
rioxxterms.typeJournal Article/Reviewen_UK
rioxxterms.versionVoRen_UK
local.rioxx.authorPrzulj, Dunja|0000-0003-1133-8835en_UK
local.rioxx.authorPesola, Francesca|0000-0002-2054-7930en_UK
local.rioxx.authorMyers Smith, Katie|0000-0003-1837-3924en_UK
local.rioxx.authorMcRobbie, Hayden|0000-0002-7777-1845en_UK
local.rioxx.authorColeman, Tim|0000-0002-7303-4805en_UK
local.rioxx.authorLewis, Sarah|0000-0001-5308-6619en_UK
local.rioxx.authorGriffith, Christopher|0000-0001-7935-8694en_UK
local.rioxx.authorWalton, Robert|0000-0001-7700-1907en_UK
local.rioxx.authorWhitemore, Rachel|0000-0002-7599-8640en_UK
local.rioxx.authorClark, Miranda|0000-0002-6179-046Xen_UK
local.rioxx.authorUssher, Michael|0000-0002-0995-7955en_UK
local.rioxx.authorSinclair, Lesley|0000-0002-2210-8181en_UK
local.rioxx.authorSeager, Emily|0000-0001-6672-5555en_UK
local.rioxx.authorCooper, Sue|0000-0002-1994-6395en_UK
local.rioxx.authorBauld, Linda|en_UK
local.rioxx.projectProject ID unknown|National Institute for Health Research|http://dx.doi.org/10.13039/501100000272en_UK
local.rioxx.freetoreaddate2024-02-16en_UK
local.rioxx.licencehttp://creativecommons.org/licenses/by/4.0/|2024-02-16|en_UK
local.rioxx.filename3042526.pdfen_UK
local.rioxx.filecount1en_UK
local.rioxx.source2046-4924en_UK
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